Canonical Allele Identifier: PA916031570
Gene: ATM HGNC NCBI

Linked Data

ClinVar Variation Id: 645300

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001338763.1:p.Gly335Glu
CA382531377
NM_001351834.2:c.1004G>A